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clindamycin phosphate
clindamycin phosphate - 59762-3728-3 - (clindamycin phosphate)
Drug Information of clindamycin phosphate
| Product NDC: | 59762-3728 |
| Proprietary Name: | clindamycin phosphate |
| Non Proprietary Name: | clindamycin phosphate |
| Active Ingredient(s): | 10 mg/mL & nbsp; clindamycin phosphate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of clindamycin phosphate
| Product NDC: | 59762-3728 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050537 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19800620 |
Package Information of clindamycin phosphate
| Package NDC: | 59762-3728-3 |
| Package Description: | 60 APPLICATOR in 1 CARTON (59762-3728-3) > 1 mL in 1 APPLICATOR |
NDC Information of clindamycin phosphate
| NDC Code | 59762-3728-3 |
| Proprietary Name | clindamycin phosphate |
| Package Description | 60 APPLICATOR in 1 CARTON (59762-3728-3) > 1 mL in 1 APPLICATOR |
| Product NDC | 59762-3728 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clindamycin phosphate |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19800620 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | CLINDAMYCIN PHOSPHATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |
